Method For Forming Dielectric Film And Method For Forming Capacitor In Semiconductor Device Using The Same

ABSTRACT

Provided is a method for forming a dielectric film in a semiconductor device, wherein the method can improve a dielectric characteristic and a leakage current characteristic. According to specific embodiments of the present invention, the method for forming a dielectric film includes: forming a zirconium dioxide (ZrO2) layer over a wafer in a predetermined thickness that does not allow continuous formation of the ZrO2 layer; and forming an aluminum oxide (Al2O3) layer over portions of the wafer where the ZrO2 layer is not formed, in a predetermined thickness that does not allow continuous formation of the Al2O3 layer

TECHNICAL FIELD

The present invention relates to a method for forming a dielectric film in a semiconductor device and a method for forming a capacitor using the same; and, more particularly, to a method for forming a dielectric film in a semiconductor device using an atomic layer deposition (ALD) method and a method for forming a capacitor using the same.

BACKGROUND ART

Recently, as the design rule of a dynamic random access memory (DRAM) has decreased, a cell region has decreased and an aspect ratio of a storage node in a capacitor has increased greatly. Thus, it has become difficult to secure a dielectric capacity required for each unit cell.

Conventionally, a dielectric film has been formed in oxide/nitride/oxide (ONO) layer structure to secure a dielectric capacity. However, recent researches on forming a dielectric film with an aluminum oxide (Al₂O₃) layer (ε=9), a hafnium dioxide (HfO₂) layer (ε=25), or a stacked layer of HfO₂/Al₂O₃, wherein the Al₂O₃ layer and the HfO₂ layer both have a high dielectric constant, have been actively progressed in attempts to secure a larger dielectric capacity. Also, such dielectric film is formed by employing an atomic layer deposition (ALD) method instead of the conventional chemical vapor deposition (CVD) method in order to respond to the large aspect ratio.

However, for a dielectric film formed with the stacked layer of HfO₂/Al₂O₃, a dielectric characteristic and a leakage current characteristic of the entire dielectric film depend on a corresponding dielectric constant ε and a band gap energy Eg of each material. That is, the dielectric film formed with the conventional stacked layer of HfO₂/Al₂O₃ shows an electrical characteristic formed by a combination of the characteristics of each layer, as described hereinafter.

Generally, a dielectric constant ε and a band gap energy Eg of the Al₂O₃ layer are 9 and 9 eV, respectively. On the other hand, a dielectric constant e and a band gap energy Eg of the HfO₂ layer are generally known to be 25 and 5.6 eV, respectively. That is, the dielectric characteristic of the entire dielectric film is affected by the HfO₂ layer, and the leakage current characteristic is affected by the band gap energy Eg of the Al₂O₃ layer. On the contrary, the leakage current characteristic of the entire dielectric film is deteriorated due to the low band gap energy Eg of the HfO₂ layer, and the dielectric characteristic of the entire dielectric film is deteriorated due to the low dielectric constant of the Al₂O₃ layer. Thus, if the dielectric film is applied in a capacitor of a DRAM device, a large limitation occurs with respect to decreasing a thickness of the dielectric film.

However, the Al₂O₃ layer functions to lower a crystallization temperature of the HfO₂ layer, which is the other layer consisting the dielectric film, and through such a function, a leakage current of the dielectric film is reduced. Therefore, in order to improve the characteristics of the dielectric film, the dielectric constant and the band gap energy of the oxide material, forming the dielectric film together with the Al₂O₃ layer, are generally required to be controlled.

DISCLOSURE Technical Problem

It is, therefore, an object of the present invention to provide a method for forming a dielectric film in a semiconductor device, wherein the method can improve a dielectric characteristic and a leakage current characteristic.

Also, another object of the present invention is to provide a method for forming a capacitor in a semiconductor device using the method for forming a dielectric film.

Technical Solution

In accordance with one aspect of the present invention, there is provided a method for forming a dielectric film, including: forming a zirconium dioxide (ZrO₂) layer over a wafer in a predetermined thickness that does not allow continuous formation of the ZrO₂ layer; and forming an aluminum oxide (Al₂O₃) layer over portions of the wafer where the ZrO₂ layer is not formed, in a predetermined thickness that does not allow continuous formation of the Al₂O₃ layer.

In accordance with another aspect of the present invention, there is provided a method for forming a dielectric film, including: forming an Al₂O₃ layer over a wafer in a predetermined thickness that does not allow continuous formation of the Al₂O₃ layer; and forming a ZrO₂ layer over portions of the wafer where the Al₂O₃ layer is not formed, in a predetermined thickness that does not allow continuous formation of the ZrO₂ layer.

In accordance with still another aspect of the present invention, there is provided a method for forming a dielectric film, including forming a [ZrO₂]x [Al₂O₃]y layer, where ZrO₂ and Al₂O₃ are mixed, x and y each representing 0 or a positive number, over a wafer using a source gas where a Zr atom and an Al atom are formed as one molecule. In accordance with a further aspect of the present invention, there is provided a method for forming a capacitor, including: preparing a substrate structure on which a contact plug is formed; forming a patterned insulation layer over the substrate structure in a manner to expose the contact plug; forming a bottom electrode over the patterned insulation layer and the substrate structure; forming a dielectric film over the bottom electrode using a method claimed in one of claim 1 to claim 27; and forming an upper electrode over the dielectric film.

Advantageous Effects

In accordance with specific embodiments of the present invention, a dielectric characteristic and a leakage current characteristic of a capacitor used in a semiconductor device can be improved by forming a dielectric film using a [ZrO₂]x[Al₂O₃]y layer, where x and y each represents 0 or a positive number. Herein, ZrO₂ and Al₂O₃ are evenly mixed in the [ZrO₂]x[Al₂O₃]y layer.

DESCRIPTION OF DRAWINGS

The above and other objects and features of the present invention will become apparent from the following description of the exemplary embodiments given in conjunction with the accompanying drawings, in which:

FIG. 1 is a flowchart illustrating a method for forming a dielectric film in accordance with a first embodiment of the present invention;

FIG. 2 is a diagram illustrating a process of forming a zirconium dioxide (ZrO₂) layer illustrated in FIG. 1;

FIG. 3 is a diagram illustrating a process of forming an aluminum oxide (Al₂O₃) layer illustrated in FIG. 1;

FIGS. 4A and 4B show diagrams illustrating a dielectric film formed through the method described in FIG. 1;

FIG. 5 is a flowchart illustrating a method for forming a dielectric film in accordance with a second embodiment of the present invention;

FIG. 6 is a flowchart illustrating a method for forming a dielectric film in accordance with a third embodiment of the present invention;

FIG. 7 is a diagram illustrating a process of forming a [ZrO₂]x[Al₂O₃]y layer illustrated in FIG. 6; and

FIGS. 8 to 10 are cross-sectional views illustrating a method for forming a capacitor in accordance with a specific embodiment of the present invention.

BEST MODE FOR THE INVENTION

Other objects and aspects of the invention will become apparent from the following description of the embodiments with reference to the accompanying drawings, which is set forth hereinafter.

First Embodiment

FIG. 1 is a process flowchart illustrated to describe a method for forming a dielectric film in a semiconductor device in accordance with a first embodiment of the present invention, FIG. 2 is a diagram illustrated to describe a sequential order of a zirconium dioxide (ZrO₂) layer formation process, and FIG. 3 is a diagram illustrated to describe a sequential order of an aluminum oxide (Al₂O₃) layer formation process.

Referring to FIGS. 1 to 3, the method for forming a dielectric film in a semiconductor device in accordance with the first embodiment of the present invention includes forming a ZrO₂ layer and then forming an Al₂O₃ layer, using an atomic layer deposition (ALD) method.

The formation process of the ZrO₂ layer is as follows. One source gas selected from the group consisting of Zr(O-tBu)₄, Zr[N(CH₃)₂]₄, Zr[N(C₂H₅) (CH₃)]₄, Zr[N(C₂H₅)₂]₄, Zr(TMHD)₄, Zr(OiC₃H₇)₃(TMTD), and Zr(OtBu)₄, is supplied inside a chamber of an ALD apparatus to adsorb zirconium (Zr) over a wafer, although not illustrated, at step S10. Herein, a temperature ranging from approximately 200° C. to approximately 350° C. is maintained inside the chamber. Subsequently, nitrogen (N₂) gas is supplied inside the chamber to purge the remaining Zr source gas, which did not become adsorbed, out of the chamber at step S11. Next, 03 is supplied inside the chamber to oxidize the adsorbed Zr over the wafer to thereby form a ZrO₂ layer at step S12. Then, N₂ gas is supplied inside the chamber to purge any non-reacted O₃ at step S13. The steps S10 to S13 are performed as one cycle T_(zr), and the cycle T_(zr) is repeatedly performed until a thickness T, of the ZrO₂ layer reaches approximately 10 Å. Herein, the reason for limiting the thickness T₁ of the ZrO₂ layer to approximately 10 Å is to form the ZrO₂ layer over the wafer W non-continuously as illustrated in FIG. 4A. During one cycle T_(zr), the thickness T₁ of the ZrO₂ layer reaches less than approximately 1 Å. Therefore, the ZrO₂ layer can be formed in a thickness nearing approximately 10 Å by repeating the cycle T_(zr) approximately 10 times.

Subsequently, an Al₂O₃ layer formation is performed. The Al₂O₃ layer formation is as follows. An Al(CH₃)₃ source gas is supplied inside the chamber to adsorb Al on the wafer in-situ at step S15. Subsequently, N₂ gas is supplied inside the chamber to purge the remaining Al source gas, which did not become adsorbed, out of the chamber at step S16. Next, O₃ is supplied inside the chamber to form an Al₂O₃ layer over portions of the wafer where the ZrO₂ layer is not formed, at step S17. As described above, when the thickness T₁ of the ZrO₂ layer is limited to less than approximately 10 Å (i.e., approximately 1 Å to approximately 10 Å), the ZrO₂ layer is non-continuously formed over the wafer W, as illustrated in FIG. 4B. Thus, the Al₂O₃ layer 2 is formed over the portions of the wafer where the ZrO₂ layer 1 is not formed, that is, between the ZrC)₂ layers 1. Subsequently, N₂ gas is supplied inside the chamber to purge any non-reacted O₃ at step S18. The steps S15 to S18 are performed as one cycle T_(Al), and the cycle T_(Al) is repeatedly performed until a thickness T₂ of the Al₂O₃ layer reaches less than approximately 10 Å. During one cycle T_(Al), the thickness T₂ of the Al₂O₃ layer reaches less than approximately 1 Å. Therefore, the Al₂O₃ layer can be formed in a thickness nearing approximately 10 Å by repeating the cycle T_(Al) approximately 10 times.

Furthermore, if a thickness Tfinal of a mixed layer including the ZrO₂ layer and the Al₂O₃ layer is smaller than a goal thickness T_(goal), then, the ZrO₂ layer formation cycle T_(zr) and the Al₂O₃ layer formation cycle T_(Al) are each repeatedly performed once at a time at steps S21 and S22. The steps S21 and S22 are repeatedly performed until the thickness T_(final) becomes substantially identical to the goal thickness T_(goal). Herein, the thickness T_(final) of the mixed layer including the ZrO₂ layer and the Al₂O₃ layer can be formed to range from approximately 30 Å to approximately 500 ÅA.

Through the above processes, the dielectric film is formed by employing [ZrO₂]x[Al₂O₃]y, where x and y each represents 0 or a positive number.

Second Embodiment

FIG. 5 is a flowchart illustrating a method for forming a dielectric film in accordance with a second embodiment of the present invention.

As shown in FIG. 5, the method for forming a dielectric film in accordance with the second embodiment of the present invention uses an ALD method like the first embodiment of the present invention. However, in the second embodiment, an Al₂O₃ layer is non-continuously formed over a wafer and then a ZrO₂ layer is formed, instead of forming the ZrO₂ layer first. Excluding such a difference, the second embodiment of the present invention is performed with substantially identical processes to the first embodiment of the present invention. Thus, detailed descriptions of the second embodiment are abridged herein for the convenience of description.

Third Embodiment

FIG. 6 is a flowchart illustrating a method for forming a dielectric film in accordance with a third embodiment of the present invention, and FIG. 7 is a diagram illustrating a formation process of simultaneously forming a [ZrO₂]x[Al₂O₃]y layer.

Referring to FIGS. 6 and 7, the method for forming a dielectric film in a semiconductor device in accordance with the third embodiment of the present invention uses an ALD method to simultaneously form the [ZrO₂]x[Al₂O₃]y layer.

A source gas such as ZrAl(MMP)₂(OiPr)₅, where Zr and Al are formed as one molecule, is supplied inside a chamber of an ALD apparatus to adsorb Zr and Al over a wafer, although it is not shown, at step S210. Herein, a temperature ranging from approximately 200° C. to approximately 350° C. is maintained inside the chamber. Subsequently, N₂ gas is supplied inside the chamber to purge the remaining source gas, which did not become adsorbed, out of the chamber at step S211. Next, O₃ is supplied inside the chamber to oxidize the Zr and Al adsorbed over the wafer to thereby form the [ZrO₂]x[Al₂O₃]y layer at step S212. Herein, the sum of x and y may be less than approximately 10.

Then, N₂ gas is supplied inside the chamber to purge any non-reacted O₃ at step S213. The steps S210 to S213 are performed as one cycle T_(Zr/Al). If a thickness T₃ of the [ZrO₂]x[Al₂O₃]y layer is smaller than a goal thickness T_(goal), then, the cycle T_(zr)/Al (S210 to S213) is repeatedly performed until the thickness T₃ of the [ZrO₂]x[Al₂O₃]y layer becomes substantially identical to the goal thickness T_(goal). Herein, the thickness T₃ of the [ZrO₂]x[Al₂O₃]y layer may be formed within a range of approximately 30 Å and approximately 500 Å.

On the other hand, although the first to third embodiments of the present invention use O₃ for the oxidation process, O₃ is one example, and H₂ 0 or oxygen plasma can be used instead of O_(3.) Also, the purge process in the first to third embodiments of the present invention use N₂ gas, N₂ is also an example, and the purge process can be performed by employing a vacuum pump or argon (Ar) gas.

Meanwhile, Tables 1 and 2 below are comparative tables to compare properties of HfO₂ and ZrO₂.

TABLE 1 Band Dielectric gap constant energy ΔEc(eV) Crystal Material (ε) Eg(eV) to Si structure(s) SiO₂ 3.9 8.9 3.2  Amorphous Si₃N₄ 7 5.1 2    Amorphous A1₂O₃ 9 8.7 2.8^(a) Amorphous Y₂O₃ 15 5.6 2.3^(a) Cubical La₂O₃ 30 4.3 2.3^(a) Hexagonal, Cubical Ta₂O₅ 26 4.5 1-1.5 Orthorhombic TiO₂ 80 3.5 1.2  Tetragonal^(a) (rutile, anatase) HfO₂ 25 5.7 1.5^(a) Monoclinic^(b), Tetragonal^(c), Cubical ZrO₂ 25 7.8 1.4^(a) Monoclinic^(b), Tetragonal^(c), Cubical

TABLE 2 Source Molecular Temp decomposition weight (1 temperature Element Name (g/mol) Torr) (° C.) Hf Hf[N(C₂H₅)₂]₄ 466.49 126 150 Hf[N(CH₃)₂]₄ 354.49 75 90 Hf[N(C₂H₅)(CH₃)]₄ 410.49 113 140 Zr Zr[N(C₂H₅)₂]₄ 379.74 108 140 Zr[N(CH₃)₂]₄ 267.22 77 80 Zr[N(C₂H₅)(CH₃)]₄ 323.22 106 130

As shown in Table 1 above, ZrO₂ has a dielectric constant similar to HfO₂, however, ZrO₂ has band gap energy relatively larger than HfO₂. That is, by using Al₂O₃-ZrO₂ in stacked or mixed layer structure, band gap energy of an entire thin film is increased, improving a leakage current characteristic of a dielectric film. Thus, it becomes easy to reduce the thickness of a dielectric film. Furthermore, if ZrO₂ is applied instead of HfO₂, it is more advantageous to apply the dielectric film in processes for a mass production because a Zr source, which can be used commercially, has a large advantage of easy handling due to extremely smaller saturation vapor pressure and molecular weight when compared to an Hf source.

Hereinafter, a method for forming a capacitor is described referring to FIGS. 8 to 10, using the method for forming a dielectric film in the first to third embodiments of the present invention. FIGS. 8 to 10 are cross-sectional views illustrating a method for forming a concave type capacitor in a dynamic random access memory (DRAM) device.

Referring to FIG. 8, a substrate 10, over which bottom layers including a storage node contact plug 18 are formed, is provided. Herein, the bottom layers 10 further include: a conductive layer 12; first to third inter-layer insulation layers 11, 13 and 17; bit lines 14; hard masks 15; and spacers 16. Herein, the conductive layer 12 is formed by employing polysilicon, and the first to third inter-layer insulation layers 11, 13 and 17 are each formed by employing an oxide-based material. Also, the bit lines 14 are formed by employing polysilicon (or titanium nitride (TiN)) and tungsten (or tungsten silicide), and the hard masks 15 are formed by employing a nitride-based material.

Subsequently, an insulation layer 19 for use in a storage node pattern is formed over the above resulting substrate structure, exposing a top portion of the storage node contact plug 18. Herein, the insulation layer 19 is formed by employing an oxide-based material or polysilicon.

Furthermore, a storage node 20 is formed over the above entire resultant structure. Herein, the storage node 20 is a bottom electrode of the capacitor, and is formed by employing one selected from the group consisting of polysilicon doped with impurities such as phosphorus (P) and arsenic (As), TiN, ruthenium (Ru), ruthenium dioxide (RuO₂), platinum (Pt), iridium (Ir), and iridium dioxide (IrO₂).

Moreover, as shown in FIG. 9, a dielectric film 21 is formed over the storage node 20. Herein, the dielectric film 21 is formed by employing [ZrO₂]x[Al₂O₃]y, where ZrO₂ and Al₂O₃ are evenly mixed, through employing one of the first to the third embodiments of the present invention. Herein, x and y each represents 0 or a positive number. For reference, the sum of x and y may be kept below approximately 10.

Next, a thermal treatment process is performed to the dielectric film 21. Herein, the thermal treatment process is performed by employing one selected from the group consisting of a furnace method, a rapid temperature process (RTP), and a rapid temperature anneal (RTA) method. Herein, the thermal treatment process is performed in an atmosphere including a small amount of Ar, N₂ or oxygen (O₂) at a temperature ranging from approximately 450° C. to 850° C.

Subsequently, as shown in FIG. 10, an upper electrode 22 is formed over the dielectric film 21. Herein, the upper electrode 22 is formed by employing a material substantially identical to the storage node 20. For example, the upper electrode 22 is formed by employing one selected from the group consisting of polysilicon doped with impurities such as P and As, TiN, Ru, RuO₂, Pt, Ir, and IrO₂.

The specific embodiments of the present invention only describe the embodiments applied to a capacitor in concave structure. However, the capacitor in concave structure is one example, and the present embodiments can be also applied to capacitors in flat and cylinder structure. Also, the embodiments can be applied as a dielectric film of a capacitor in a radio frequency (RF) device. Furthermore, the embodiments can be applied to a dielectric film interposed between a floating gate and a control gate in a memory device including a flash memory, an electrically erasable programmable read only memory (EEPROM), and an erasable programmable read only memory (EPROM).

The present application contains subject matter related to Korean patent application No. 2004-0110920, filed in the Korean Intellectual Property Office on Dec. 23, 2004, the entire contents of which is incorporated herein by reference.

While the present invention has been described with respect to certain preferred embodiments, it will be apparent to those skilled in the art that various changes and modifications may be made without departing from the scope of the invention as defined in the following claims. 

1. A method for forming a dielectric film, comprising: forming a zirconium dioxide (ZrO₂) layer over a wafer in a predetermined thickness that does not allow continuous formation of the ZrO₂ layer; and forming an aluminum oxide (Al₂O₃) layer over portions of the wafer where the ZrO₂ layer is not formed, in a predetermined thickness that does not allow continuous formation of the Al₂O₃ layer.
 2. The method as recited in claim 1, wherein the forming of the ZrO₂ layer includes forming the ZrO₂ layer in a thickness ranging from approximately 1Å to approximately 10 Å that does not allow continuous formation of the ZrO₂ layer.
 3. The method as recited in claim 1, wherein the forming of the Al₂O₃ layer includes forming the Al₂O₃ layer in a thickness ranging from approximately 1 Å to approximately 10 A that does not allow continuous formation of the Al₂O₃ layer.
 4. The method as recited in claim 1, wherein the dielectric film being a mixed layer of the ZrO₂ layer and the Al₂O₃ layer is formed to have a thickness ranging from approximately 30 A to approximately 500 Å.
 5. The method as recited in claim 1, wherein the forming of the ZrO₂ layer includes: supplying a zirconium (Zr) source gas inside a chamber of an atomic layer deposition (ALD) apparatus to adsorb the Zr source gas over the wafer; supplying an inert gas inside the chamber or using a vacuum pump to purge the Zr source gas which did not become adsorbed; supplying an oxidation gas inside the chamber to oxidize the adsorbed Zr source gas to form the ZrO₂ layer; and supplying an inert gas inside the chamber or using a vacuum pump to purge any non-reacted oxidation gas.
 6. The method as recited in claim 5, wherein the forming of the ZrO₂ layer is repeatedly performed within a range of forming the ZrO₂ layer to a predetermined thickness that does not allow continuous formation of the ZrO₂ layer over the wafer.
 7. The method as recited in claim 5, wherein the forming of the ZrO₂ layer comprises using: the Zr source gas that includes one selected from the group consisting of Zr(O-tBu)₄, Zr [N(CH₃)₂]₄, Zr [N(C₂H₅) (CH₃)]₄, Zr [N(C₂H₅)₂]₄, Zr(TMHD)₄, Zr(OiC₃H₇)₃(TMTD), and Zr(OtBu)₄; the inert gas that includes one of argon (Ar) and nitrogen (N₂); and the oxidation gas that includes one selected from the group consisting of water (H₂O), ozone (O₃), and oxygen plasma.
 8. The method as recited in claim 5, wherein the forming of the ZrO₂ layer is performed at a temperature ranging from approximately 200° C. to approximately 350° C.
 9. The method as recited in claim 1, wherein the forming of the Al₂O₃ layer includes: supplying an aluminum (Al) source gas inside a chamber of an ALD apparatus to adsorb the Al source gas over the wafer; supplying an inert gas inside the chamber or using a vacuum pump to purge the Al source gas which did not become adsorbed; supplying an oxidation gas inside the chamber to oxidize the adsorbed Al source gas to form the Al₂O₃ layer; and supplying an inert gas inside the chamber or using a vacuum pump to purge any non-reacted oxidation gas.
 10. The method as recited in claim 9, wherein the forming of the Al₂O₃ layer is repeatedly performed within a range of forming the Al₂O₃ layer to a predetermined thickness that does not allow continuous formation of the Al₂O₃ layer over the wafer.
 11. The method as recited in claim 9, wherein the forming of the Al₂O₃ layer comprises using: the Al source gas that includes Al(CH₃)₃; the inert gas that includes one of Ar and N₂; and the oxidation gas that includes one selected from the group consisting of H₂O, O₃, and oxygen plasma.
 12. A method for forming a dielectric film, comprising: forming an Al₂O₃ layer over a wafer in a predetermined thickness that does not allow continuous formation of the Al₂O₃ layer; and forming a ZrO₂ layer over portions of the wafer where the Al₂O₃ layer is not formed, in a predetermined thickness that does not allow continuous formation of the ZrO₂ layer.
 13. The method as recited in claim 12, wherein the forming of the ZrO₂ layer includes forming the ZrO₂ layer in a thickness ranging from approximately 1 Å to approximately 10 Å that does not allow continuous formation of the ZrO₂ layer.
 14. The method as recited in claim 12, wherein the forming of the Al₂O₃ layer includes forming the Al₂O₃ layer in a thickness ranging from approximately 1 Å to approximately 10 Å that does not allow continuous formation of the Al₂O₃ layer.
 15. The method as recited in claim 12, wherein the dielectric film being a mixed layer of the ZrO₂ layer and the Al₂O₃ layer is formed to have a thickness ranging from approximately 30 Å to approximately 500 Å.
 16. The method as recited in claim 12, wherein the forming of the ZrO₂ layer includes: supplying a Zr source gas inside a chamber of an ALD apparatus to adsorb the Zr source gas over the wafer; supplying an inert gas inside the chamber or using a vacuum pump to purge the Zr source gas which did not become adsorbed; supplying an oxidation gas inside the chamber to oxidize the adsorbed Zr source gas to form the ZrO₂ layer; and supplying an inert gas inside the chamber or using a vacuum pump to purge any non-reacted oxidation gas.
 17. The method as recited in claim 16, wherein the forming of the ZrO₂ layer is repeatedly performed within a range of forming the ZrO₂ layer to a predetermined thickness that does not allow continuous formation of the ZrO₂ layer over the wafer.
 18. The method as recited in claim 16, wherein the forming of the ZrO₂ layer comprises using: the Zr source gas that includes one selected from the group consisting of Zr(O-tBu)₄, Zr[N(CH₃)₂]₄, Zr[N(C₂H₅) (CH₃)]₄, Zr[N(C₂H₅)₂]₄, Zr(TMHD)₄, Zr(OiC₃H₇)₃(TMTD), and Zr(OtBu)₄; the inert gas that includes one of Ar and N₂; and the oxidation gas that includes one selected from the group consisting of H₂O, O₃, and oxygen plasma.
 19. The method as recited in claim 16, wherein the forming of the ZrO₂ layer is performed at a temperature ranging from approximately 200° C. to approximately 350° C.
 20. The method as recited in claim 12, wherein the forming of the Al₂O₃ layer includes: supplying an Al source gas inside a chamber of an ALD apparatus to adsorb the Al source gas over the wafer; supplying an inert gas inside the chamber or using a vacuum pump to purge the Al source gas which did not become adsorbed; supplying an oxidation gas inside the chamber to oxidize the adsorbed Al source gas to form the Al₂O₃ layer; and supplying an inert gas inside the chamber or using a vacuum pump to purge any non-reacted oxidation gas.
 21. The method as recited in claim 20, wherein the forming of the Al₂O₃ layer is repeatedly performed within a range of forming the Al₂O₃ layer to a predetermined thickness that does not allow continuous formation of the Al?O₃ layer over the wafer.
 22. The method as recited in claim 20, wherein the forming of the Al₂O₃ layer comprises using: the Al source gas that includes Al(CH₃)₃; the inert gas that includes one of Ar and N₂; and the oxidation gas that includes one selected from the group consisting of H₂O, O₃, and oxygen plasma.
 23. A method for forming a dielectric film, comprising forming a [ZrO₂]x[Al₂O₃]y layer, where ZrO₂ and Al₂O₃ are mixed, x and y each representing 0 or a positive number, over a wafer using a source gas where a Zr atom and an Al atom are formed as one molecule.
 24. The method as recited in claim 23, wherein the forming of the [ZrO₂]x[Al₂O₃]y layer includes having the sum of x and y less than approximately
 10. 25. The method as recited in claim 23, wherein the dielectric film being a mixed layer of the ZrO₂ layer and the Al₂O₃ layer is formed to have a thickness ranging from approximately 30 Å to approximately 500 Å.
 26. The method as recited in claim 23, wherein the forming of the [ZrO₂]x[Al₂O₃]y layer comprises using the source gas that includes ZrAl(MMP)₂(OiPr)₅.
 27. The method as recited in claim 23, wherein the forming of the [ZrO₂]x[Al₂O₃]y layer includes: supplying a source gas where a Zr atom and an Al atom are formed as one molecule, inside a chamber of an ALD apparatus to adsorb the source gas over the wafer; supplying an inert gas inside the chamber or using a vacuum pump to purge the source gas which did not become adsorbed; supplying an oxidation gas inside the chamber to oxidize the adsorbed source gas to form the [ZrO₂]x[Al₂O3]y layer; and supplying an inert gas inside the chamber or using a vacuum pump to purge any non-reacted oxidation gas.
 28. A method for forming a capacitor, comprising: preparing a substrate structure on which a contact plug is formed; forming a patterned insulation layer over the substrate structure in a manner to expose the contact plug; forming a bottom electrode over the patterned insulation layer and the substrate structure; forming a dielectric film over the bottom electrode using a method claimed in one of claim 1 to claim 27; and forming an upper electrode over the dielectric film.
 29. The method as recited in claim 28, further comprising performing a thermal treatment process to the dielectric film after the dielectric film is formed, wherein the thermal treatment process is performed in an atmosphere of Ar, N₂ or oxygen (O₂) at a temperature ranging from approximately 450° C. to approximately 850° C. 